1361132-19-5

Basic information

• Product Name: 1',3'-dimethyl-3-phenyl-3,4-dihydro-1H,1'H-spiro[anthracene-2,5'-pyrimidine]-2',4',6'(3'H)-trione
• CAS NO: 1361132-19-5
• Molecular Weight: 398.461
• Mol File: 1361132-19-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1',3'-dimethyl-3-phenyl-3,4-dihydro-1H,1'H-spiro[anthracene-2,5'-pyrimidine]-2',4',6'(3'H)-trione(CAS DataBase Reference)
• NIST Chemistry Reference: 1',3'-dimethyl-3-phenyl-3,4-dihydro-1H,1'H-spiro[anthracene-2,5'-pyrimidine]-2',4',6'(3'H)-trione(1361132-19-5)
• EPA Substance Registry System: 1',3'-dimethyl-3-phenyl-3,4-dihydro-1H,1'H-spiro[anthracene-2,5'-pyrimidine]-2',4',6'(3'H)-trione(1361132-19-5)

Safety Data

• Hazardous Substances Data: 1361132-19-5(Hazardous Substances Data)

Upstream product

• 536-74-3 phenylacetylene 
• 288402-18-6 methyl 3-(trifluoromethanesulfonyloxy)naphthalene-2-carboxylate 

Relevant articles and documents

Rapid access to 3-aryltetralin skeleton via C(sp3)-H bond functionalization: Investigation on the substituent effect of aromatic ring adjacent to C-H bond in hydride shift/cyclization sequence

The concise construction of 3-aryltetralin skeleton via hydride shift mediated C-H bond functionalization was achieved. In this process, the benzylic [1,5]-H shift occurred smoothly to furnish tetralin derivatives in good to excellent chemical yields. The electronic and steric properties of the aromatic ring adjacent to the C-H bond influenced significantly the reactivity of this transformation.